Results 71 to 80 of about 5,762 (257)

Ebstein anomaly and Trisomy 21: A rare association

open access: yesAnnals of Pediatric Cardiology, 2014
This is a case report of a patient with Trisomy 21 with Ebstein anomaly, a ventricular septal defect, and acquired pulmonary vein stenosis; a rare combination, diagnosed during a routine neonatal examination.
Stephanie L Siehr   +3 more
doaj   +1 more source

Zero Fluoroscopy Ablation of Arrhythmias in Patients With Congenital Heart Disease

open access: yesJournal of Arrhythmia, Volume 41, Issue 6, December 2025.
Zero‐fluoroscopy radiofrequency ablation using 3D electroanatomic mapping was performed in 42 patients with mild, moderate, or great complexity congenital heart disease. Acute success was 100%, with no complications and minimal recurrence over 48 months. This approach eliminates radiation exposure while maintaining safety and efficacy across select yet
Shailendra Upadhyay   +4 more
wiley   +1 more source

Partial PFO Closure for Persistent Hypoxemia in a Patient with Ebstein Anomaly

open access: yesCase Reports in Cardiology, 2015
Ebstein anomaly is characterized by deformities of the anterior leaflet of the tricuspid valve and atrialization of the right ventricle. Patients with severe tricuspid regurgitation are recommended to have tricuspid valve surgery with concomitant atrial ...
S. A. Zuberi   +5 more
doaj   +1 more source

Experience of medical treatment of neonates with Ebstein anomaly in the intensive care unit

open access: yesAlʹmanah Kliničeskoj Mediciny, 2018
Background: Neonates with Ebstein anomaly may remain a  challenge for neonatal intensive care units due to continuously changing clinical manifestations.
M. V. Tarayan   +2 more
doaj   +1 more source

Right Atrial Aneurysm after Chest Trauma: Late Presentation [PDF]

open access: yes, 2012
Relata-se o caso de um paciente de 59 anos de idade, com história de traumatismo torácico grave com fratura de vários arcos costais aos 20 anos, com início recente de cansaço e palpitações, a quem foi detetada taquicardia auricular, convertida ...
Branco, LM   +7 more
core   +1 more source

Transcatheter Management of Severe Paravalvular Leak in the Inferior Vena Cava Prosthesis of the TricValve Bicaval Valve System

open access: yesCatheterization and Cardiovascular Interventions, Volume 106, Issue 5, Page 2945-2948, November 1, 2025.
ABSTRACT We present a 74‐year‐old female with a history of mechanical aortic and mitral valve implantation and non‐Hodgkin lymphoma. She presented with right sided heart failure due to severe functional tricuspid regurgitation and was treated with transcatheter TricValve bicaval system implantation.
Marcel A. Beijk   +2 more
wiley   +1 more source

Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study [PDF]

open access: yes
Previous studies have shown that over 40% of babies with Down syndrome have a major cardiac anomaly and are more likely to have other major congenital anomalies.
Addor, Marie-Claude   +29 more
core   +1 more source

Hypoalbuminaemia predicts outcome in adult patients with congenital heart disease [PDF]

open access: yes, 2015
Background In patients with acquired heart failure, hypoalbuminaemia is associated with increased risk of death. The prevalence of hypoproteinaemia and hypoalbuminaemia and their relation to outcome in adult patients with congenital heart disease (ACHD ...
Alonso-Gonzalez, R   +11 more
core   +1 more source

Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long‐Standing Clinical Utility of FISH

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT While the standard diagnostic test for suspected 22q copy number disorders is by chromosomal microarray, this case highlights the importance of utilizing FISH to localize allelic copy number when there is a family history of deletion/duplication syndrome for accurate recurrence risk assessment.
Laura M. Bryant   +5 more
wiley   +1 more source

Ethnical variations in the incidence of congenital heart defects in Gorgan, Northern Iran: A single-center study [PDF]

open access: yes, 2014
Background: Congenital heart disease (CHD) is the most common congenital anomaly in newborns. This study was performed to determine the live birth incidence of CHD by ethnicity and sex in Gorgan, Northern Iran.
Golalipour, M.J.   +4 more
core  

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